Amneal Pharmaceuticals is hiring for the position of Officer, Quality Assurance at its pharmaceutical manufacturing location in Visakhapatnam, Andhra Pradesh. The role focuses on quality assurance, cGMP compliance, manufacturing process monitoring, quality documentation, deviation management, and regulatory compliance.
Candidates with an M.Sc. in Chemistry and relevant experience can review the eligibility criteria and apply through the company’s careers portal.
Job Details
| Particulars | Details |
|---|---|
| Company | Amneal Pharmaceuticals |
| Job Title | Officer, Quality Assurance |
| Job ID | 8654 |
| Job Category | Quality Assurance |
| Qualification | M.Sc. Chemistry |
| Experience | 1–4 years |
| Job Location | Visakhapatnam, Andhra Pradesh |
| Job Type | Full-time |
| Posting Date | 14 October 2026 |
| Application Deadline | 20 October 2026 |
| Work Location | Plot No. 68, JNPC, Visakhapatnam, Andhra Pradesh – 531019 |
Positions
- Position: Officer, Quality Assurance
- Department: Quality Assurance
- Location: Visakhapatnam, Andhra Pradesh
Responsibilities
The selected candidate will support pharmaceutical quality assurance activities, including:
- Defining and maintaining quality activities, processes, and standards in accordance with current Good Manufacturing Practices (cGMP).
- Monitoring manufacturing processes and product outputs against internal quality standards and regulatory requirements.
- Maintaining quality systems, procedures, policies, and inspection programs.
- Supporting in-process quality monitoring and quality-related interactions with vendors.
- Reporting and troubleshooting manufacturing deviations and finished-product defects.
- Compiling Annual Product Quality Review (APQR) reports and maintaining quality documentation.
- Supporting compliance with 21 CFR Parts 210 and 211.
- Assisting with change control and deviation management.
- Participating in complaint and recall assessments.
- Supporting the implementation of corrective and preventive actions (CAPA).
Eligibility and Qualifications
Candidates should meet the following criteria:
- Educational Qualification: M.Sc. in Chemistry.
- Experience: 1–4 years of experience.
- Domain: Pharmaceutical quality assurance and manufacturing quality processes.
Required Skills
Applicants should have knowledge or skills in the following areas:
- Quality Assurance
- Audit and Inspection Preparedness
- CAPA and Deviation Oversight
- Change Control Documentation
- Data Integrity and Documentation Security
- Document Review and Approval
- Documentation and Record Control
- Good Documentation Practices (GDP)
- Quality Risk Analysis and Control
- Regulatory Compliance
